کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
5598256 1574188 2017 9 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
A Femoral Common Vein Aneurysm in a Patient with Neurofibromatosis Syndrome Type 1
ترجمه فارسی عنوان
رانی مشترک ورید آنوریسم در یک بیمار مبتلا به سندرم نوروفیبروماتوز نوع 1
موضوعات مرتبط
علوم پزشکی و سلامت پزشکی و دندانپزشکی کاردیولوژی و پزشکی قلب و عروق
چکیده انگلیسی
Neurofibromatosis type I (NFI), also called Von Recklinghausen disease, is an autosomal dominant disease secondary to a genetic mutation on the long arm of chromosome 17. This disorder affects neural crest cells. Cutaneous clinical forms are the most frequent with multiple benign skin neurofibromas, associated with café au lait skin spots and iris hamartomas. Vascular abnormalities in NF1 are rare but have also been well described. The most frequent abnormalities are characterized by arterial aneurysm degeneration, stenosis, and malformations. Venous locations are rare, but some cases of venous aneurysms were described with ruptures as complications. We present a rare case of thrombosed venous femoral aneurysm associated with a pulmonary embolism in a patient affected by NF1.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Annals of Vascular Surgery - Volume 40, April 2017, Pages 299.e7-299.e9
نویسندگان
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